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Minerva Pediatrica
|
January 15, 1981
[Grisel's syndrome in childhood]
G Pinelli, M Piantanida, A Roffo, et al.
Journal of Medical Genetics
|
July 1, 1989
Differential expression of the ICF (immunodeficiency, centromeric heterochromatin, facial anomalies) mutation in lymphocytes and fibroblasts
P Maraschio, R Tupler, E Dainotti, et al.
Genes, Chromosomes & Cancer
|
January 1, 1990
Gene dosage effect in acquired monosomy 7: distinct behaviour of beta-glucuronidase and phosphoserine phosphatase
A Minelli, M Piantanida, E Maserati, et al.
AJR. American Journal of Roentgenology
|
November 1, 1994
Hepatic vascular malformations in hereditary hemorrhagic telangiectasia: imaging findings
E Buscarini, L Buscarini, G Civardi, et al.
Journal of Medical Genetics
|
June 1, 1996
Hereditary haemorrhagic telangiectasia with extensive liver involvement is not caused by either HHT1 or HHT2
M Piantanida, E Buscarini, C Dellavecchia, et al.
Prenatal Diagnosis
|
November 1, 1992
Prenatal diagnosis of metabolic diseases on chorionic villi obtained before the ninth week of pregnancy
A Minelli, M Piantanida, G Simoni, et al.
Human Genetics
|
October 1, 1990
Deletion of specific sequences or modification of centromeric chromatin are responsible for Y chromosome centromere inactivation
P Maraschio, O Zuffardi, A Caiulo, et al.
Mutation Research
|
June 1, 1993
Frequency of chromosomal aberrations after exposure to gamma-radiation of human chorionic villi
R Salvi, C De Andreis, S Pariani, et al.
Journal of Healthcare Education and Training : the Journal of the American Society for Healthcare Education and Training
|
March 6, 1987
Linking theory to practice: the research challenge facing health care educators
M Piantanida, H Glazer-Waldman, K Linnell, et al.
European Annals of Allergy and Clinical Immunology
|
May 21, 2026
Efficacy and safety of mepolizumab in hypereosinophilic syndrome
L M Losappio, J Moll, H S Mousa, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 31) with videos related to
Sort By:
Page
of 4
Minerva Pediatrica
|
January 15, 1981
[Grisel's syndrome in childhood]
G Pinelli, M Piantanida, A Roffo, et al.
Journal of Medical Genetics
|
July 1, 1989
Differential expression of the ICF (immunodeficiency, centromeric heterochromatin, facial anomalies) mutation in lymphocytes and fibroblasts
P Maraschio, R Tupler, E Dainotti, et al.
Genes, Chromosomes & Cancer
|
January 1, 1990
Gene dosage effect in acquired monosomy 7: distinct behaviour of beta-glucuronidase and phosphoserine phosphatase
A Minelli, M Piantanida, E Maserati, et al.
AJR. American Journal of Roentgenology
|
November 1, 1994
Hepatic vascular malformations in hereditary hemorrhagic telangiectasia: imaging findings
E Buscarini, L Buscarini, G Civardi, et al.
Journal of Medical Genetics
|
June 1, 1996
Hereditary haemorrhagic telangiectasia with extensive liver involvement is not caused by either HHT1 or HHT2
M Piantanida, E Buscarini, C Dellavecchia, et al.
Prenatal Diagnosis
|
November 1, 1992
Prenatal diagnosis of metabolic diseases on chorionic villi obtained before the ninth week of pregnancy
A Minelli, M Piantanida, G Simoni, et al.
Human Genetics
|
October 1, 1990
Deletion of specific sequences or modification of centromeric chromatin are responsible for Y chromosome centromere inactivation
P Maraschio, O Zuffardi, A Caiulo, et al.
Mutation Research
|
June 1, 1993
Frequency of chromosomal aberrations after exposure to gamma-radiation of human chorionic villi
R Salvi, C De Andreis, S Pariani, et al.
Journal of Healthcare Education and Training : the Journal of the American Society for Healthcare Education and Training
|
March 6, 1987
Linking theory to practice: the research challenge facing health care educators
M Piantanida, H Glazer-Waldman, K Linnell, et al.
European Annals of Allergy and Clinical Immunology
|
May 21, 2026
Efficacy and safety of mepolizumab in hypereosinophilic syndrome
L M Losappio, J Moll, H S Mousa, et al.
Page
of 4